Label: FIRST STREET ANTIBACTERIAL LIQUID HAND- benzalkonium chloride liquid

  • NDC Code(s): 61504-551-01, 61504-551-02, 61504-551-16, 61504-551-17, view more
    61504-551-64
  • Packager: Amerifoods Trading Company
  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated January 30, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENT

    Benzalkonium Chloride........0.13%

  • Purpose

    Antiseptic

  • Uses

    For hand sanitizing to decrease bacteria on the skin.

  • Warnings

    For external use only.

  • When Using this Product

    Avoid contact with the eyes.

    In case of eye contact, flush eyes with water.

    Stop use and ask a doctor if irritation or redness develops

    or if condition persists.

  • Keep out of reach of children.

    If swallowed, get medical help

    or contact Posion Control Center right away.

  • Directions

    -Apply small amount of product to wet hands

    -Work into lather and rinse thoroughly

    -Dry hands

  • Inactive Ingredients

    Aloe Barbadensis Leaf Juice, Caprylyl/Capryl Glucoside, Citric Acid, Cocamide MIPA, Cocamidopropyl Betaine, Fragrance, Glycerin, Lauryl Polyglucose, Magnesium Nitrate, Maltodextrin, Methylchloroisothiazolinone, Methylisothiazolinone, PEG 150 Distearate, FD&C Red #40, Tetrasodium EDTA, Water, FD&C Yellow #5

  • First Street Antibacterial Hand Soap

    image description

  • INGREDIENTS AND APPEARANCE
    FIRST STREET ANTIBACTERIAL LIQUID HAND 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61504-551
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE.13 kg  in 100 kg
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    WATER (UNII: 059QF0KO0R)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61504-551-021 in 1 BOX01/30/2024
    1NDC:61504-551-013.80564 kg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:61504-551-171 in 1 BOX01/30/2024
    2NDC:61504-551-16.0568 kg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    3NDC:61504-551-641.91 kg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/30/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/30/2024
    Labeler - Amerifoods Trading Company (626388680)
    Registrant - Amerifoods Trading Company (626388680)
    Establishment
    NameAddressID/FEIBusiness Operations
    Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.028311595manufacture(61504-551) , api manufacture(61504-551) , pack(61504-551)